Archive for the ‘Blindness’ Category

Reid My Mind Radio – The Blind Temptations

Wednesday, April 12th, 2017

EVERY NOW AND THEN I SHARE some of THE THINGS THAT CROSS MY MIND.

In this episode , I’m pointing out the fact that things that should help  us can be the same things that do more than distract us from our goals!

TRANSCRIPT

Show the transcript


TR:
The title of this episode, “The Blind Temptations”, may have you thinking I am announcing my new idea of
touring with four other gentlemen who are blind and singing the classics, like My Girl, Papa Was a Rolling Stone, Just My Imagination.

Notice I didn’t include Ain’t too Proud to Beg in that song list.

Maybe you now have images of the famous Motown group doing their dance routines either while holding white canes or guide dogs.

If so, well you’re stupid!.
[Laughs]

No I’m just kidding! you’re probably just silly!

I’m not really talking about those Temptations.

Before I get into that…
[Audio: temptations…. hold up!]
[Audio: rmmradio Theme]

TR:
The Temptations I am referring to are scary to me.

That’s not something I would ever expect to hear myself say out loud and especially here on my podcast, but  it’s true!

Temptations lure a person away from staying on track.

They offer temporary  distraction, a fantasy for something that most likely cannot be attained.

For those going through vision loss or any significant life change; these distractions can be much more tempting.

Think of those who experience sudden job elimination that requires a whole new approach to employment while in mid-career.

Confidence levels are down. Self-identities are challenged.

In such examples, many distractions are accepted in our society or at least they’re understood

Think of the classic I just got fired story.

It’s usually the guy working at the factory for years.  He shows up at the bar after getting the news. He gets a drink on the house first and then his buddies begin buying rounds.

go ahead, get your drink on, you deserve it. the poor guy!

When it comes to adjusting to blindness, there’s a lowering of the bar that takes place. People expect less from the person experiencing the loss. . More than often, it’s those outside of the immediate family. Some times that could include those inside the personal circle or family and friends.

And then let’s not forget that much of the misunderstanding about blindness and what that means for a person could be inside the individual experiencing the loss. They may now limit themselves. Their expectations are impacted and often that means becoming satisfied with less.

“Well, you can’t work so you will now stay home and listen to your radio all day.”

I felt temptations early on after my own loss. When I realized it, it shook me up.

I was in my mid-thirties. I wouldn’t say I was on my way to becoming CEO or even Manager, but I was growing in my career and
reaching some personal and career goals.

My first reaction to vision loss was to push through.

My sight was basically already gone and I had a surgery  scheduled for the end of January, that I knew would leave me permanently blind. Yet, I thought in my mind that I would be back at work by the end of February at the latest.

I find that so funny now!

I didn’t think  about the new things I would have to learn. I didn’t think about issues of accessibility because I simply wasn’t aware of them at that time. My focus was just on continuing where I left off. I didn’t really give that much thought into how would I do things or
even if those things I used to do would still matter to me.

Soon after the temptations began doing the things they do…

[Audio: Temptations, “The Way You Do The Things You Do”]

The first seems almost common today; addiction.

This has always been a fear of mine. ! I have addictive tendencies.
Yes, right now to things like chocolate… I go through binge periods.

I’m not making fun of addiction in any way. I know today addiction to pain killers is looked at quite differently from
let’s say how addictions were viewed when crack was the drug of choice! The substance, shouldn’t matter nor should who the addicts are but that’s another episode topic.

I was given Percoset for the pain following my surgery. I found myself taking them nightly. I soon began noticing a smell after I would ingest the pill.
It didn’t stink nor did it smell good. There was a sweetness to the smell, but
not like candy, cake or chocolate!
Thank goodness because I would be somewhere fiending right now!

It was different.

I began noticing the smell during the day when I didn’t take  the pill. I wasn’t anywhere near the pill.
I’d start thinking about taking the pill and the way it lulled me to sleep. That numb feeling of no pain, worries or problems that seemed of any immediate importance. I soon realized I was taking the pill without even any pain.
it was more about the habit of taking it and the way it carried me away to sleep at night.

It picked me up and placed me on a bed of clouds and off to sleep I went.

When I smelled the scent of the pills during the day I started thinking about  how I now had a pass. Taking the pills to  help relieve me of the nonphysical pain seemed almost acceptable. I began creating  what seemed like reasons that would permit the behavior…

“Well, I’m not working now, I’m alone in the house today.”

“The doctors gave me the pills, I have to use them.”

These were just mental excuses. I was  arguing with myself internally as to why I should take a pill even though I had no physical pain.

“who’s gonna know?”
That was it!  I flushed the rest of the pills and that was the last time I took them.

Temptations come in all forms!

During my first few months of adjusting, I would spend the early part of the day before noon, watching a lot of standup comedy on comedy central.

Stand up is great! It’s mostly accessible as it is usually vocal performances.
It was helpful, it took me out of my own head and made me laugh. That energy release helped me feel a bit more positive.

During that time my television options were limited. I didn’t have much in the way of audio description for television or movies. I didn’t enjoy the movie watching experience unless
I was watching something familiar and
I’m not really the type who likes re-watching a lot  of things.

I think about the access we now have to Netflix and
other options for audio described movies and television.
that could have played into my adjustment.
I could have chosen to spend my time mindlessly watching television or movies all day.

I can hear the excuses in my head now!

“What else am I supposed to do?”

“Watching and analyzing shows or movies gives me some insight into humanity and maybe even my own situation.”

“I’ll watch the movie while I fold the laundry.”

Right now, with shows like Black Mirror on Netflix? I might accept having that bar lowered. Sitting around playing with my iPhone and watching Netflix all day sounds pretty good!

“Don’t do it!”

It’s not just Netflix!

There’s the internet and technology in general too! You know these are real temptations!

At one point it looked like blind people would be barred  from participating in so much of this technology. However, rightfully  so, accessibility improvements are happening. Are they happening fast enough for everyone?
No, but they are happening and we have to acknowledge that.

Even console game makers are thinking inclusively and developing games
that will enable gamers with disabilities including blindness to participate.

I’m not mad at that or any of these “temptations.”

I guess I’m speaking especially to those adjusting to vision loss and who want to make a point of reaching their own goals with their new situation.

The more access we have to things that can improve our opportunities and daily lives the better. It just so happens that these things are potentially the same things that can tempt us into complacency and accepting less of ourselves.

In a way though, isn’t that what accessibility is all about?

Access not only to participate, but to make all of our decisions that affect our lives.

Like choosing to subscribe to this podcast! The show is short in duration! It won’t take you away from  anything. You can fit it in on a quick break or as you’re doing your daily activities; making or eating breakfast, lunch or dinner.  Brushing your teeth. Walking your dog. Whatever it is you do, doing it is better with Reid My Mind Radio!

Subscribe anywhere  you get podcasts.

Shout out to the person who left me a review on iTunes.

I hear that’s the way to help get other people to discover the show. If you can please give me a review as long as it’s good.

No seriously if you are a hater, feel free to hate, but everyone knows haters shouldn’t rate, just discriminate!

I’m good with that!

[Laughs]

Thanks for listening!
[Audio: RMMradio theme]
Peace!

Hide the transcript

Reid My Mind Radio – Certain Victory

Wednesday, March 29th, 2017

Occasionally, I come across a story that I think fits into a specific category. This latest piece for example was supposed to be about Robert Ott, a blind entrepreneur, but it ended up as so much more.

Picture of Robert Ott

Adjusting to blindness, disability  or any significant life change takes real strength, courage and spirit. Hear how Robert fought back from trauma to become a successful entrepreneur in the Business Enterprise Program.

Hit play to start listening, then subscribe to the podcast and tell a friend!

 

 

Resources

Transcript

Show the transcript

TR:
What’s good everyone!

In this episode I’m bringing you another piece produced for Gatewave Radio.
If you don’t know they are the radio reading service  out of New York City.
their purpose is to provide access to printed materials to those who are print impaired.
Meaning blind or visually impaired, or
for other reasons like physical or cognitive disability, they can’t read print.

Yes, many people today have access to technology that eliminates the need for this service, but
there are still a lot of people who either cannot afford or learn the technology.

One of the things I have realized over the last few years is that I really appreciate telling other people’s stories.

I’m also realizing it’s getting time for me to take another step.

To really tell some one’s story you have to spend time getting to see who they really are and what they are all about.

Doing that, takes a budget.
All of my productions are best described as NMO & NMI…
No Money Out & No Money In!
Well definitely NMI…
If you factor time and equipment well there’s a cost.

I’m honestly not sure what the next step is for me.

I guess I am just letting the universe know I am ready … or
at least open to taking a new step in telling people’s stories for a purpose.

Let’s get into this story and then some more immediately following the Gatewave piece.

But first…
[Audio: RMMRadio Theme Music]

&********

RO:
My name is Robert J. Ott. I originally graduated the Business Enterprise Program  in the state of New Jersey. I then became recertified in the state of Washington and moved my life out here and became a blind entrepreneur in this program.

TR:
The Business Enterprise Program  or B E P
is a federally authorized program implemented  by each state and territory in the United States.

they train and license   people who are blind or visually impaired
to establish and operate food service businesses in
public and private facilities.

RO:
That business did the food services for the western regional center of the National Oceanic Atmospheric  Administration. it was about  a thousand people in the complex. I took over the day care center, I fed 52 kids a day, overseeing 48 vending machines. We did all the catering; breakfast, lunch, fancy dinners . We used to get liquor permits from time to time for international meetings that we’d have there. I spent 10 years of my life there.

TR:
During a Washington state meeting of  B EP vendors,
Robert learned about an opportunity to gain a military contract.
Such contracts were never awarded to a blind vendor in the state and
only 35 vendors in the country had ever received such lucrative opportunities.

Feeling as though he reached a peak in his business at that time,
Robert decided he would pursue the contract.

After 2 and a half years of legal battles with the department of defense ,
Robert was awarded the contract.

RO:
I formed a corporation; it was titled Certain Victory Food Services Incorporated. I had 833 employees.

September 1, 2004 I walked into my office on what is now called  Joint Base Lewis McChord. We were providing the labor, proper service; we were taking care of these young men and women for fighting  for freedom and independence.

TR:
Robert success story can be defined by one word; Pilsung.

The definition, is in his story,
beginning with his introduction to the Martial Arts.

Growing up in Southern New Jersey.  Robert was raised by a single mom.

Like most boys who first watched Bruce Lee on the big screen,
Robert immediately began imitating the acrobatic moves.

[Audio: Bruce Lee’s fighting scene]

RO:
I wasn’t sure what I was doing. My brain wasn’t even doing the thinking. My body was simply kicking  and moving, punches and everything else.

TR:
Robert’s mom couldn’t afford to send her son to lessons.

When Robert turned 12, an affordable and convenient opportunity was presented and
he began studying Tae Kwon Do

RO:
I ended up  winning the New Jersey State Championships two years in a row. From there, the Junior Olympics down in Florida, The Fight for Cancer Championships, Northeast Pocono Championships Garden State Championships. I also lost some battles too. What it was really doing on the inside was  building my self-esteem and confidence to look somebody eye to eye and shake their hand with warmth, goodness and my own self security confidence  at the same time.

TR:
Robert continued studying different forms of Martial Arts with
multiple instructors in New Jersey and Pennsylvania.

Each instructor providing something new,
One in particular stood out to Robert.

RO:
I remember opening up Tae Kwon Do Times magazine. In the back was the directory  of instructors and little pictures of their faces. And it was one in Pennsylvania  and I said this is the guy I need to go to. And I remember my girlfriends said what are you talking about. I said, he’s looking at me. And she laughed. I said no he is. There I met Grand Master  Go Chae Teok. I became one of his students. A year following that I became the officer manager and chief  instructor . I began to operate, run and dealt with sales instructing, maintenance, advertising, marketing and the biggest thing that happened during that time is that here I am  standing in front of a group of 60 children with all of the parents up on the second floor loft looking down  and I’m teaching. Or I’m standing in front of all of these adults that are much older than me and here I am their instructor and they’re looking to me for guidance. Here I am in the office when people would come in with challenges they’d have in life and we’d be talking. I began to realize more than anything  else that I  do this from the heart and I’m good at what I do . It’s a passion I had. I was 18 years old.

TR:
By 1990, Robert was running his own school teaching Hapkido.

RO:

Which is a Korean Martial Arts. It translates to art of coordinated power. It was growing. So much was going with my life. A lot of responsibility, my relationship was being challenged, I had a great business but I was still trying to figure out how am I going to get everything to tie in together and make ends meet. I’d just given my mother away at her wedding. She married a beautiful man  and my mother gave birth to a beautiful baby boy. This is when I was 21 years old.

TR:
On October 6, 1990 Robert’s life would change forever.

RO:
It’s funny because all that night, I kept saying to myself over and over again you’re not gonna go out, you’re not gonna go to this bar. I couldn’t shut my mind down I had to do something and I guess going there was that answer at the age of 21.

[Audio: Sounds of bar crowd]

So I went in, I was chit chatting, this and that, it was no more than 10 minutes  later a large group of people came in who were heavily intoxicated. I was talking to a female , we were having a nice conversation and the next thing you know another individual  came between us and was getting involved, he wanted to put his hands on her.

She’s with me, I think you had a little bit too much to drink.

She went towards the back of the bar and I was slowly putting on my jacket  to go back to the end of the bar  to walk away from the situation. I certainly could defend myself  and take care of myself but I also learned in life that when you’re dealing with people in certain situations  they could be 1 inch tall and you may be in the best shape of your life but if they don’t care about life  you’re dealing with a whole other ball game!

As I was walking away he pushed me from behind . I turn around to defend myself. The next thing you know, the manager of the bar  was pushing me out the door . The bouncer was pushing the other guy out the door and it was all just happening.

I remember very little, but the key parts I do remember is my right leg going between his legs and sweeping his feet off the ground. Dropping my knee into his groin and I was on top of him. And then the next thing I remember I was tucking my shirt in with my friend in front of me. The door cracked back open  that went out to the parking lot and the  man while I was looking the other direction put a gun to my head and pulled the trigger.

[Audio: Gunshot, followed by ambulance…]

The bullet entered the left part of my skull  and went through the left temporal lobe of my brain. Caught the nerve to my left eye , destroyed my taste and smell and blew up in my right eye.

They got me over to Cooper Trauma Center which is located in Camden New Jersey. It was a total of 17 hours  that I laid there and it was nothing they could do.

TR:
Robert wasn’t expected to survive.
His mother was told if he did it was almost certain that he would have severe brain damage.

RO:
A nurse by the name of Fran Orth  who worked in the Trauma Center came in on the second shift. She spent time reading my information looking at me, reading information, looking at me,  she began to question why wasn’t my head lifted up. Why was not this done, why was not that  not done. And the Neuro Surgeon said there’s nothing we can do he’s going to be dying. She said but did you call Dr. Luis Servante?

TR:
Dr. Servante received the call and answered.
He went on to perform surgery that gave Robert another chance at life.

Recovery, would take some time.

He had to deal with Meningitis that required another stay in the hospital.

At the time of the shooting, Robert was a fit 185 pounds.
As a result of the fall after being shot
Robert’s jaw was broken and wired shut.
He dropped to about 125 pounds.

RO:
I couldn’t believe this was happening to me. Everything was racing through my mind. I’ve got pictures of me doing dive rolls over large groups of people and doing splits in the air. I used to go running a lot on the beach and hand springs and just all kinds of beautiful great stuff. I was so weak I couldn’t even do a push-up and now I’m blind. I can’t get around, my independence, my confidence, my self-esteem, my balance.

TR:
The recovery wasn’t just physical.

As the owner and operator of a Martial Arts school,
Robert was more than just an instructor to his students.

RO:
My school was still operating. My students were keeping it going for me, but I was embarrassed to go back. I didn’t want the children and people to see me now. I was ashamed of myself. I could have taught you ten different way when someone puts a gun to you. Techniques and things and ways of taking them down and removing the gun from their hands etc. How your body moves and how your eyes are and how you react to it.

I never thought it would really really happen!

TR:
It was Martial Arts that would once again  help Robert find his way.

RO:
Richard Kemon was my very first Martial Arts Instructor. I really looked up to him, respected him so much. He was like a father to me. And he said Bobby you have to put your uniform on, you gotta go back to your school.

TR:
Robert would go on to regain his  self-confidence and seek out new opportunities.

When it was time, he learned of the BEP program.

RO:
I remember this guy came by the house  to bring me a watch, a talking watch from the New Jersey Commission of the Blind. We started talking about the Business Enterprise Program. I decided to investigate it more. It was what I wanted to do, my dream, but I didn’t look at it as my dream. I looked at it as my tool.

TR:
This was just one tool of many.

Robert already had tools he began accumulating  when introduced to the Martial arts.

I’m talking about more than  the
flying kicks or wood shattering punches.

RO:
Working with people with self-control, confidence, peace of mind, communicating properly, sharing your energy and spirit.

TR:
That spirit eventually guided Robert to Washington state.
Fortunately, he didn’t leave his  sense of humor behind.

TR [In conversation with Robert]:
What made you go from Jersey all the way to Seattle?

RO:
Well that’s a lot of times what  happens when you’re blind and get behind the wheel.

TR:
[Laughs…]
Nice!

TR:
In addition to becoming a successful entrepreneur, he began once again teaching Martial Arts and more…

RO:
I started getting involved with working with other individuals who are blind. I put together a women’s self-defense seminar. I spent time with he Wounded Warriors. I got involved with the children at the Elementary School. I wrote a book.

TR:
The name of that book?
Certain Victory, which is also the name of Robert’s company.

Once again, it goes back to the martial arts; it goes back to pilsung!.

RO:
That same magazine that I told you I was reading when I told you I saw the picture of Grand master Goh.

The article I read in that magazine was called Pilsung. It was about a man and he just earned his first degree black belt.

TR:
Soon after, while piloting his own plane, he crashed.

RO:
And he ended up hitting the high tension line; wires. And 90percent of his body was burnt and he survived.

The whole story  was about overcoming this, getting through this, fighting the fight, finding what he called certain victory. In Korean, pilsung means certain victory through strength, courage and indomitable spirit.

TR:
One word, two syllables Pilsung  helped one man strive to reach his potential.

Robert’s book, Certain Victory is available on Bookshare.org.
It’s also available on Amazon.com and his website Certain Victory.com.

This is Thomas Reid
[RO:
There’s one in Pennsylvania and I said this is the guy I need to go to.]

for Gatewave Radio
Audio for Independent Living.

[Audio Bumper]

Some of my favorite conversations here on Reid My Mind Radio are with those who are adjusting to Blindness.
Notice I didn’t say adjusted.
I truly believe the adjustment process is a continuing practice.

If you ever talked to anyone experiencing blindness or disability,
you may have heard stories about body snatchers and mysteriously disappearing people.

Ok, I’m not being literal.

These are the people in our lives who no longer come around or
they just act very differently around us…

Robert says this was one advantage of making the move out west.

RO:
Nobody knew me here from when I could see.
Thomas the other issue I battle with is I was very well known when I could see. And every time I turned around I’d run into somebody in the supermarket or in the store and they were just always saying to me we’re so sorry for what happened Robert. But they were getting together with me anymore. They weren’t the friends they used to be. I was not the same Robert  any more. I was not the same Bobby. I was somebody different.

Out here I was who I was . No more nor less. people know me for who I am right now. It was almost like breaking free.

TR [In conversation with Robert]:

Yeh, a lot of people kind of fade away. They fade away! It is what it is!

RO:
They do!

TR [In conversation with Robert]:

That ability to start fresh really sounds nice!

RO:
Yes, there’s several components Thomas that I think have been  what I have grabbed onto to help recreate and or clarify who and what I am right now. And in so many words I am the same guy I always was. You know when we were younger all we wanted to do was know, know, know. Learn more and learn more  and learn more. And as I’ve gotten older I’m now trying to understand , understand  and understand more more more!

TR:
Those things that we want to know when we are younger and
try to understand more when we’re older
are said to always be inside us.

That idea that Robert talked about, Pilsung or
strength courage and  Indomitable spirit.
These are already inside of us and
we just need to believe that and
find our way of accessing especially
when we experience life changes.
It’s not easy, but hearing from people like Robert and others, it’s worth the effort.

I don’t know my next step in producing this podcast,
stories for Gatewave or any other outlet  or
even other things I tend to focus my energy on…

But I do know as Robert said…

RO:
Hey if it makes a difference  for one person in this world Thomas then we win!

You can win too!

Subscribe to Reid My Mind Radio in your favorite podcast app…
just look for Reid My Mind Radio… remember that is R E I D.

You can also listen via the Stitcher or Tune In Radio app.

Check out ReidMyMind.com for links, all past episodes plus more.

Big thanks to Robert for sharing his story.
Thanks to riley Gibson for recording Robert’s side of the conversation.
Thanks to you for listening!

[Audio: RMMRadio Outro Theme]

Peace!

Hide the transcript

Reid My Mind Radio: Doctor Dre’s The Fight Back

Wednesday, March 15th, 2017

Picture of Doctor Dre, seated with a tan fur jacket with the caption, Doctor Dre The Fight Back!

Doctor Dre of Yo MTV Raps, NYC’s Hot 97 Morning Show, the movie Who’s the Man? And so much more … is launching The Fight Back!

Diagnosed with Type 2 Diabetes and now blind, this fight back is about more than you probably think.

This episode features the piece produced for Gatewave radio followed by more personal conversation with Dre. Plus, you know there’s only one way to intro this podcast… if you were a morning show listener you know I had to do it…it’s the roll call!

So c’mon yawl, listen to Dre…
>scroll down a bit, , to hear the show press play!

 

Resources:

 

Transcript

Show the transcript


TR:
What’s good everybody?
This is a special episode so I’m going to jump right in…
it’s no mystery , the title of the episode says it all.

If you’re in my age group You remember when older folks said rap was a fad and
black radio didn’t play the music!

You remember when MTV played videos and they weren’t black artists let alone rap music.

Yes, this episode is featuring that Doctor Dre from YoMTV Raps and many other things like the Hot 97 morning show.
With that in mind! There’s only one way for me to kick-off the podcast…

Yeah, I’m gonna do it!

[Audio: From The Hot 97 Morning Show with Ed, Lisa & Dre
Music…
“What’s up yawl, whatcha got to say, who’s on the phone with Ed, Lisa & Dre?”]

TR:
Yo, TReid’s the name, and right now’s the time
Welcome to the podcast called Reid My Mind!

Cheah!

[Reid My Mind Intro]

TR:
Significant vision loss can force a person to face real doubts and questions.
Such as;
Why did this happen to me?
What do I do now?

Andre Brown has chosen to answer the last question by launching a fight;
well really a fight back.

It’s more than vision loss.

In  2008 Andre was diagnosed with type 2 Diabetes.

He experienced multiple complications of the disease including Charco – foot Syndrome which he says can cause a collapse of the ankle.

DD:
My vision loss came as a progression of that and not taking care of myself properly.

my vision loss was a gradual thing where I  started seeing little things across my vision. Little lines and you know things jumping.

TR:
After These lines often called floaters,  multiple surgeries to repair detached retinas,
Andre was left with some light perception.

DD:
Diagnosed as Diabetic Retinopathy but  as the Doctor said  to me , he said that’s what’s   blocking your vision, you have scar tissue in the back. He said we can’t do anything about  it until we stop the Diabetes. So once that happens then  we can do a different procedure or two to see if we can make the sight  come back.
I’ve spoken with a lot of different people and everyone has told me that my sight  returning is a very strong possibility, especially with what I am doing now.

TR:
What he’s doing now?
Simply put, he’s fighting back!

This fight is just as much for others as it is for himself.

Andre’s in a unique position to take on this job.
You see he’s been working in support of the careers of others for years.

Andre Brown, is better known as Doctor Dre, a pioneer  in Hip Hop culture and entertainment.

Starting out in WBAU, the Adelphi University radio station in Long Island,
Doctor Dre would eventually go on to record music with his group Original Concept.

He D Jayed for the Beastie Boys.

He was involved in getting one of Hip Hop’s most prolific and influential groups, Public Enemy on to Def Jam records.

Most people know him as part of the Ed Lover and Doctor Dre Duo who
hosted “Yo MTV Raps” every weekday
between 1989 and 1995; As well as
extremely successful radio morning shows in New York City between 1993 and 1998.

DJ, musician, actor, author… and now
Doctor Dre is  in a position to bring real attention to two of today’s
very significant health crisis ;
Diabetes & Vision loss.

DD:
Well we have the program that’s called Doctor Dre’s The Fight Back.

Taking the situation and being able to talk to other people and say, I can show you through  what I’m going through  that we all can change. We all can grow.

I’m finding other people that have different or similar experiences and being able to share that. So the fight back is
how do we reach out and get so many resources to work with you to try to actually change your situation.

TR:
Changing the situation by providing access to information  including;
medical, lifestyle and technology.

DD:
I’m doing a lot of Holistic medicine along  with traditional medicine to work with my Diabetes  and just to change my diet. Just putting that under better control

I’m playing the Guinea pig so everyone can  see it.

TR   [In conversation with Dre]
When you say   you’re playing the Guinea pig what does that mean?

DD:
Sometimes you have to go out and someone has  to go oh hey does that work, well I’ll try it  let’s see

I’m not bringing guarantees, I’m trying to bring choices.

What we’re doing is trying to bring those choices to the fore front. so there no longer just whispered in a corner or you have to pull this up on the Google thing… know we’re gonna say no, here’s a bunch of things here, find a way to find something that works best for you. Here are some things that are very easily at your beck and call.

And when you have options, there’s so much more you can do.

TR:
Real life style changes that affect the way we think about nutrition.

DD:
And that’s one of my goals in The Fight Back, is to change bad thinking.  The mother of 4 who works three  jobs with four kids and they have to run to McDonald’s because they  want those Happy Meals; I want to change the Happy Meal to a life meal.

TR:
Lifestyle choices are like adjusting to vision loss; it’s personal.

DD:
you do what you feel the most comfortable doing  and you work from that position. Everybody’s an individual about it. There’s no one magic thing for one person. There’s a lot of great things out there and I  am discovering those things to help  me accomplish doing other things. I’m very open to learning.

TR [In Conversation]:
What types of things are you discovering?

DD:
I have a phone I could talk to and it  speaks and dials  and talks to me.

The technology now is catching up. I believe like Netflix has where they actually have  a program that is designed so when you’re watching a program it describes everything so you get the full affect.
I’m discovering it one at a time but I don’t know the name of everything I just go wow that exists , that’s a good idea, that’s a really good idea.

TR [In Conversation with Dre]:
that’s Audio Description.

DD:
Yes.

TR [In Conversation with Dre]:
Just for full disclosure, I’m blind myself.

DD:
Oh, ok!

TR [In Conversation with Dre]:
The experience is unique and different for everyone. So I’m trying to gauge what is your experience and how other people can relate and learn… whatever that is because that’s what experience is all about. There for everyone.
DD:
Exactly.

Well with me I understood simply when it was starting to happen  I said don’t panic.
I’ve become a person that reaches for solutions. And rather than falling into , oh my god I can’t believe this is happening  and go into depressed mode I said no  this may happen, this is what you may need to prepare to start doing. And I started preparing myself for it. I said you know what I said you know what  this may be, but darkness  won’t last forever. I said  you have God behind you  and God has already told you  this isn’t forever, this is to slow you down  this is just to make sure  that you can listen and hear what I have to say. And I started listening and hearing what he had to say  more than I started talking.

I embrace it. And in embracing it he has put me on a path  to help other people and to reach out and express myself not  just about the type 2 Diabetes not only about the blindness but  about when something goes on and there’s a struggle sometimes embrace your struggle to find your solutions.
It doesn’t mean it’s a guarantee for a cure or a guarantee to a perfect answer  but what it does is says you know what  I’m more than what’s going on with me.
I can also work with this.

If you have a good relationship with your family, friends and  other people and reaching out. I learn every day from so many different people  and I pay attention and I  try to pass on some of the knowledge of what I get  so that people can help themselves

TR:
The Fight Back is a give and take; a collaboration.

TR [In conversation with Dre]:
So what is The Fight Back, what does that look like? in the world. Is that like a  web portal

DD:
It’s going to be a website… we’re building as we speak because I didn’t want to just put something out there … like it’s easy to say we’re going to do that  and throw it out there and  people just think that’s it, that’s it… no so I said , first thing we’ll do  is I’ll go out and start talking , build different interviews up and now it’s starting to take different testimonials  from different people  and it’s attached to other situations  also , you know I’m working with  a friend of mind from a company called Rally Wing and they had family who had diabetes and their discussing stuff with me.

Another gentlemen by the name of Marvin Mizell who is Jam Master Jay’s brother  has a company called JMJ Foundation  for the youth. He has Sickle Cell and Diabetes so connecting with his thing. there’s a bunch of people that I have connected with  and I said you know what maybe I should be that focal point to bring people together. and see if we can actually work, not just to a cure and better treatments ,but to better understanding  and better conversations

So going out now and talking to different people and listening to what their saying  how they fought back
that’s what this fight back is all about.

Bring those stories to light.
Bring this action to light!
And be a little educational, be a little entertaining, be informative, and be supportive
That’s where the strength is!

TR [In conversation with Dre]:
Is the reality show still a thing?

DD:
We went out there we talked to different places, everyone was excited, yeh we want to do this, yes Dre we love it. And as more we kept talking, my idea disappeared and it became this other thing. It was like that’s not what we’re talking about .

I have a little experience in creating television programs.
We’re creating our own show. Creating our own messaging, making our own venue because the technology allows us to do this.

How do we take all these different instances and work together. Instead of just having a website, a page, you know do this  and get this. No, I want you to come on, I want you to see these different testimonials to be able to reach out to like you and to say hey I want you to talk to him because your experience can help some other people. Your conversation can help someone else who may be feeling down and go hey wow it isn’t as bad as I thought or it could be really bad so we’re going to try and reach out. Go see people shake hands, kiss babies, do whatever needs to be done. We’re going to run the ultimate campaign! The campaign of life of wellness and happiness. That’s a campaign where you just can’t be elected. there is no electoral college for that!

TR [In conversation with Dre]:
[Laughing!!]

DD:
I’m sorry! I’m so sorry!

TR [In conversation with Dre]:
Don’t apologize for that. That’s real!
[Laughing!]

DD:
My things are based on love
People want to sit back and talk about this guys this and this one’s that. Hate, hate!
I said, you know what man, hate carries weight! With love you can soar!
And I got nothing but love man!

TR:
When the site is completed, you will be able to learn more at Doctor Dre TFB.com.

There’s a quote I like to refer to that’s attributed to a Greek philosopher or motivational speaker depending on who you believe…
It’s not what happens to you, but how you react to it that matters.

Doctor Dre,  reacting with love
to make information more easily available , bring
health choices to the forefront,  create a place where
others can share their experiences, all while
remaining faithful and encouraging;

In this fight, there can be only one winner; nothing but love!

This is Thomas Reid, for Gatewave Radio;

Inserted from DD:
“Bring those stories to light. Bring this action to light! And be a little educational, be a little entertaining.”

Audio for independent living!

[Audio: Dre drop a load on em’, from “You down with MTV”]

TR:

Podcasts allow for longer exploration and intimate conversation.
In a way, I hinted to this in the Gatewave story edit.

There’s power in conversation between two people
exchanging knowledge about their shared experience.

Some things you really only feel comfortable talking about with someone who you know gets what you’re saying.
You don’t want to have to explain yourself.

The conversation could just be two people kicking around philosophical ideas.

often it’s , just talking about real practical sharing of information.
Like when Dre mentioned posting to Facebook:

DD:
One of my friends growing up he said I saw you on Facebook and I’m going how is he doing this? Isn’t he blind? And he’s like, he’s actually posting and doing this and that… I said, I have somebody doing that. The way I post is my son posts for me. He’ll put stuff up  that I need written or said or whatever we want to put on my Facebook page. So that’s fine. That’s how that works.

TR [In conversation with Dre]
You could do it yourself too you know right?

DD:
Please, I’m listening

TR [In conversation with Dre]
Ok so you have the iPhone and the app on the iPhone is , I mean it’s all accessible. It sounds like you mainly probably use Siri, the dictation?

DD:
Yes, I use Siri right now.

TR [In conversation with Dre]
So  you don’t use the keyboard at all, you never tried to use the keyboard?

DD:
No!  (Surprised!)

TR [In conversation with Dre]
Oh, you can absolutely. Do you have Voice Over turned on?

DD:
You know what,  I’ve been trying to go to the Apple store to sit there and have them explain everything that can be done , I do not probably have it turned on, no.

TR [In conversation with Dre]
Ok!

TR:
Sometimes we assume that people are supposed to just know things…
Those who do, need to be more open and welcoming in order to make that information available.
At the same time remain open to receiving new ideas.

Three words that tell me Dre is going to be fine
no matter what the end result of his vision loss turns out to be;

DD:
“Please, I’m listening!”

TR:
Please, I’m listening!

Dre doesn’t know me.
He’s been around the world and has access to people and privilege.

DD:
Having reached out to people like Stevie Wonder.

TR:
Now, who am I to challenge something that Stevie says. I only say that because what Stevie means to me.

Adjusting to blindness though, is different from living with blindness all your life.

For example, I grew up only seeing out of one eye.
The challenge to me was different compared to someone who loses an eye
later in life and never had monocular vision.
I could share some information about things they should know,
but prior to blindness I wouldn’t have been able to relate to that loss.
That adjustment is the challenge. Growing up only knowing one thing is a different experience.

Meanwhile, I too could probably benefit from some of their discoveries.

Dre knows there’s so much more to learn and is open to that information for himself and others.

Our conversation though, went deeper.

Like when I wanted  Dre to know about an aspect of blindness
that is experienced and the ramifications that are felt by too many.

TR [In conversation with Dre]

We started the conversation with a little bit about  blindness and with the things people do and do not know, right. There’s all this technology, there’s so much you know going on and one of the big big issues  when it comes down to the blind community . The image of people who are blind in terms of how that’s perceived in society,  there’s a lot of negative connotation when it comes to blindness that I realized that I had and as I met other people  you know, blind at birth or blind afterward, there’s an incredible resource out here that is not being taken advantage of. So within the blindness community and within the disability community, unemployment is 70 percent.

DD:
Yes, it is!

TR:
So many people don’t even understand that. Even in just in terms of how people can do things and the abilities that are there it’s just not known. In part of what you’re doing you may not have or may have thought about it, you are going to be a representative  of that to some degree. Whether or not you like it or not, right, people are going to look at you and they now look you as he’s blind and therefore when they think of other people who are blind they will think of you. And so the things that you’re doing are going to send a positive message  not only to people who are sighted but also to other people who are blind who may have  bought into that.

I just ask you to ponder that, you know!

DD:
I hear what you’re saying. It’s very funny that you say those things. Funny not laughing wise, funny as it’s very interesting how we do that … I now the same way  I was put upon  and told do you believe you can get your sight back, I’m going to ask you those questions to… do you believe you can get your sight back?

TR:
Now, I had lots of people say they were hoping and praying I get my sight back, but
No one outside my immediate family has ever directly asked me that question.

I know a lot of people might think that question shouldn’t have been asked.
But it was part of our conversation so in no way was I offended or upset by that. This was a conversation between two people experiencing vision loss.

This isn’t some random person asking me on the street.

My answer and Dre’s response forced me to think about how I look at that question.

My answer… next time on Reid My Mind Radio!

[Laughing….]

Just playing!

TR [In conversation with Dre]
Nah! My situation is totally different.

DD:
Mmm hmmm!

TR [In conversation with Dre]
Number 1 my cancer is a genetic cancer. I was born  with a cancer called Retinoblastoma. I lost my left eye  as a child. The tumor overtook that eye.  I had at that time, this was in 68, well 69, radiat5ion. Thirty five years later that radiation caused another huge tumor  to grow in the back of my right eye and so I had no real choice because it was right on the optic nerve and so when it’s on that optic nerve, the next step is the brain So my choice was do I take that out  and live? Now mind you my wife was pregnant with our second child, we just moved from the Bronx to the Poconos in a house… so my right eye was removed.  There’s no coming back from that.

DD:
Ahh, yes.  You can’t get an eye transplant?

TR:
No, there’s no such thing as an eye transplant. The amount of nerves  that are in the eye  is unlike any place else. But that’s ok!  I didn’t have a choice and that’s ok, you know because I  my family, I have my little girls you know and so  my thing was like you  stepping back from the industry, my thing was I’m raising my girls you know. I’m a keep working and do whatever I can and be a  you know a help to other people  be a you know, productive member of society  and all of that and I can do that when I’m blind. I like to say the only thing I can’t do is drive.

DD:
Well that tells me a funny story that  I thrown out to Stevie Wonder about doing a movie I used to tell when I was doing interviews and I still do but know people go like you’re really going to do that and I said yeah I’m going to do that. I was being interviewed and they said Dre you gonna do any more movies and I said yeah I’m going to do movies. I said right now I’m in conversation with Stevie Wonder , we’re doing this movie called Just Drive the Damn Bus! And everyone fell out. They said for real. I said yeah and in that movie you’re going to see  Stevie and I drive the bus.

TR:
Uh huh!

DD:
They were like, how are you going to do that?  I said that’s the point, you gotta see the movie. And I was joking about it right?And then I started working with  one of my partners and we started  coming up with a concept of the movie and  it was like, this could work. I said, it’s a movie! I said, but do you understand what would happen and he said  but how are you guys going to act in the movie? I said  the same way other people act  in a movie, you hit your mark, you say your lines you keep moving, that’s not an issue.

TR:
Right.

DD:
Stop making an issue of a non-issue.  And then I told, a matter of fact I told  I was talking to LL Cool j and I told him about it and he  fell out laughing. He said you’re serious. I said I’m dead serious, your gonna do that.
I don’t walk around with dark glasses on. My son says Dad put the glasses on  stop walking around… I said no people need to see my eyes the way they are. So what, it doesn’t matter.
I say this to say this to you. We may not know the technology that will exist to help you gain sight when you need it, but I believe in my heart with what you just told me and what just trinkled through me is you and I our meeting is not coincidental  and I can’t promise this, but I just have this feeling  in my gut you’re gonna get your sight, because you need to see your kids.

TR [In conversation with Dre]
[Exhales!]

DD:
I know you’re saying, how can that be done? I don’t know. I don’t have that answer yet. That answer may come next year, that may come in five years, we don’t know. When I put those goals in front of me  it gives me something to shoot for. Reality or not, that’s why I say  that thing about the movie,  just drive the damn bus… Bill said, you are nuts, you’re outta you… I said no I’m not. I said because we can do anything if you put your mind to it.  Remember seeing Star Trek the Next generation

TR [In conversation with Dre]

yeah, yeah, with Jody…

DD:
LaVar Burton! He put on a visor and  he could see. But when he went to do the movies  LaVar didn’t want that visor on his face they pulled it off and put something on his eyes…we don’t know what’s coming!

TR [In conversation with Dre]
Right!

DD
Now if I could get in a DeLorean and go sixty years forward and grab it and pull it back  and say here put this on it works

TR [In conversation with Dre]
[Laughing….]

DD:
I don’t know!

TR [In conversation with Dre]

Right, right!

DD:
But we’re back to what the Fight Back is all about, choices!

TR [In conversation with Dre]

What you just said  helped me because the obstacles in front of me are not  necessarily just based on sight. And that goes into a really deeper conversation, but when you said  you get something from  that, there’s no way  I would want to take that away from you!

TR:
I’m not a dream killer and never want to be that!

Believing in the ability to regain sight doesn’t mean  not believing in the abilities of people who are blind.

Often though, that seems to be the message we hear from different organization in their fight against blindness.

The NY Times a few weeks ago ran an article with the headline;
The Worst that Could Happen? Going Blind, People Say
The article itself discussed some of the fears, and ways to prevent or slow
certain types of eye diseases, but
it did nothing to help ease that fear for
those who are facing  that in their present or future.

That’s not cool!

They only looked at vision loss from the medical perspective  ,
prevent the disease and there’s no longer an issue!

But there’s the society side!

That fear is what leads to people not wanting to in anyway associate themselves with blindness.
That fear and miseducation leads to that 70 percent unemployment.

But Dre’s not saying that.
His approach appears to be inclusive, holistic as in a full picture.

He’s straight up keeping his options open
I can support that!

Let’s do some shout outs!

First of all Doctor Dre,
thank you brother for the conversation,
for the courage and willingness to bring options to the people!
I hope to hear more about the Fight Back in the near future.

These next two shout outs come with a recommendation…
Audio: The Cipher Show theme[]

If you are a hip hop fan and like to hear background stories
from artists, journalists and those on the business side…
you need to check the cipher show.
Host Shawn Satero was kind enough to help make this interview happen.

It’s one of my favorite podcasts.

At least once every episode you will hear a person being interviewed say, Wow, you really did your research!”

you’ll hear it at least once an episode which lets you know it’s a quality show.

Shout out to Shawn and the Cipher show!

Shout out to Bill Adler who helped coordinate this with Dre.
BTW, Sir, please continue producing that Christmas  Mix Tape,
my daughter and I look forward to that Cipher episode each year.
No comments folks, I like the different cultural Christmas music and I ain’t ashamed to say it!

If your listening right now on Sound Cloud hit that follow button.
You can subscribe  via any podcatcher on your phone or tablet,
Apple, Android it doesn’t matter we’re outchere!

We’re on Stitcher and Tune In.

Got feedback?
Hit me at reidmymindradio@gmail.com … Remember Reid, is R E I D.

Thanks for listening!

Peace!

Hide the transcript

 

Reid My Mind Radio – Who is Joe Capers

Wednesday, February 15th, 2017
A picture of Joe Capers, an African American man seated on a couch staring into the camera with sunglasses!

Joe Capers

En Vogue, Tony Tony Tone and more musical artists from Oakland could help answer this question. In this  episode we meet two gentlemen creating a documentary that will help others do the same.

The second part of today’s podcast explores Hip Hop from two angles you may have not known existed.
* Krip Hop Nation, an international network for artists with disabilities.
* Hip Learning,  using the rap element of Hip Hop to help children learn science and more!

So stop what you’re doing
Prepare to hear the words they say
The only way to do it…
Press on the button that says Play!

… Oh snap, #Bars son!


Subscribe & Follow


Resources

  1. Alternative Minds
  2. Krip Hop Nation
  3. The Best of Krip-Hop Nation on CD Baby

4. Hip Learning

Transcript

Show the transcript

TR:
What’s good family!
Happy Black History Month to everyone…
even if you don’t feel that’s something you celebrate or even really acknowledge.
The simple truth, if you are on this planet,
chances are great that you have been impacted by African American people. There’s so much from the world of invention, science and culture. An unfortunately, that’s not discussed during the other 11 months of the year.

Today’s episode includes a recent piece for Gatewave Radio that shows how sometimes people are like pieces in a puzzle. If one piece is missing, that full puzzle can never be complete.

Following the Gatewave piece you will hear more from two brothers who in their own way are expanding Black history. And ,  making sure we know, that includes people with disabilities.

Are You ready?
[Audio: “I know you’re gonna dig this!”]
[RMMRadio Intro]

[Audio Mix: “En Vogue, Tony Tony Tone, Digital Underground and MC Hammer!]
TR:
Today, the question, Who is Joe Capers?

In the 1980’s and 90’s  artist’s like , En Vogue,
Tony Tony Tony,
Digital Underground,
MC Hammer
all had a few things in common.
They all were based in Oakland,
each made their way to the top of the charts
and Joe Capers.

In order to find out who is Joe Capers,
I spoke with two gentlemen from California’s Bay Area.
First up, Leroy Moore, originally from the east coast, raised in Connecticut and New York City.

LM:
I’m an activist, journalist and author. I also started what’s called Krip-Hop Nation with a K. It’s an international network of musicians with disabilities. My disability is Cerebral Palsy. I had it since birth.

I found out about Joe Capers when I was doing radio. KpFA out here  in Berkley. They had a radio show about people with disabilities. Joe Capers was blind African American man here in Oakland in the 70’s, 80’s and 90’s. He had one of the first accessible home studios at that time.
TR:
That’s a full recording studio in the basement of his home. All sorts of Oakland artists from MC Hammer to En Vogue and others you may have never heard of recorded at Joe’s studio

Leroy learned of another person who could help further answer the question… who is joe capers?

Naru:
I got a call from Leroy one day, he said “Naru you knew Joe Capers?” I was like yeah Joe?

TR:
Meet Naru Kwina , an Oakland California  based artist and teacher. .

Naru:
Joe was just the coolest guy with the biggest smile.
Joe played the base, the drums the keyboards so he was a master musician.

TR in conversation with Naru:
Was Joe doing more of the production? Was he just kind of the studio owner? What was he actually doing?
***

Naru:
Listen brother! His studio was called “J-Jams Studio: Joe did everything.  He had his mix board in Braille. He recorded, he engineered he mixed, he produced. He did everything that you could every possibly do in the studio. And he had the greatest ear I have ever been around and I’ve  been doing music over 40 years of my life. If you had one note or one little thing off he knew and he would call you on it. You know because he was blind you thought you’d  get away with stuff.

TR:
Joe was a professional and  demanded that those  in his studio acted the same. Naru, who is also a rapper, and went by the name Quick back then, recalls the time when Joe instructed him to memorize his lyrics and not use written notes in the recording booth.

Naru:
I’m in the booth one day and I had my little paper… like nah he ain’t gonna know… [laughs] he was like bruh, I could hear the paper rattling in the booth. And he sent me home. He sent me home and told me not to come back until I knew my lyrics.

So he was really dedicated to the music and that dedication is still with me and when I started having my own studio and production I always said nope don’t come in here with no paper, learn your lyrics.
[Laughs] So I got that from Joe!

TR:
Learning more about Joe, Leroy was surprised others didn’t know him.

LM:
Oh my god, this man needs to be recognized in Oakland because he really changed the Oakland sound of Hip-Hop and Soul.

TR:
During that conversation between Naru and Leroy the idea was sparked.

Naru:
When I said you know somebody outta do a film about Joe, he [Leroy] said why don’t you do it. I said man, I’m not a film maker man… he said but  yeah you know people. Reluctantly, I took that upon myself.

TR:
there’s lots involved in the process.

Naru:
I just contacted people who had cameras, mics and I had to contact all the artists. I literally probably have  6 or 7 hours of interviews. Everybody from MC Hammer, Digital Underground, Dwayne Wiggins from Tony tony Tone and other people who just knew Joe on a personal level or recorded with Joe… who were closer with Joe. Some of the more interesting interviews are from people you would never heard about who Joe touched in a particular  way. I could just say that he’s still here with us because all the people he touched and how many people still  think about Joe.

TR:
What began as a 15 minute documentary about the career of Joe Capers has morphed into much more. Running his own studio known as J-Jams wasn’t solely a business venture. This was back in the error when recording music professionally required significant investment.
Large studios charged hundreds of dollars an hour for studio time.

Naru:
Joe was changing like between $20 or $25 an hour r. The quality of sound was on par with anything coming out of these big studios. Joe knew the music that we were doing.  He understood it better than some of the engineers who were  in these big studios who were used to . doing rock music or folk and country. Joe  understood the R&B  and the Hip-Hop… the need for that bottom.

TR:
While the music might be about that base, for Joe it included the chance to offer help and encouragement.

Naru:
He was also a teacher. He would take young kids off the street from time to time. Some people were actually living with him. He would teach young kids  to engineer. Pretty much gave at least  two people I know roofs over their heads until they got their act together. They might have been out doing some street business and he didn’t really want that.  So he was trying to teach people another way to make money and be successful.

LM:
Joe Capers taught newly blind people independent living skills.

TR:
Making a documentary takes a lot of patience and research. It also takes creativity. Not only in the traditional sense as in the filming and writing, but also in the approach to resolving real  challenges that inevitably arise.

In order to make up for a lack of video footage of Joe and artists in the recording studio, original animation is being incorporated into the film.

And I am pleased to report that plans are included for audio description, making the film more accessible to those with vision loss.
When complete the film will be distributed by way of local public television, online, film festivals and live screenings.
Events developed around the release of the film will include a live concert focusing on emerging artists including those with disabilities. The concert will be an annual event taking place in August. in Oakland, this now has significant meaning.

Naru:
I wouldn’t say we, I helped but Leroy was the most instrumental…

LM:
Every August is now Joe Capers month in Oakland. That’s the first  Black Disabled man that’s been recognized  by the city of Oakland.

TR:
Here’s how you can help contribute to the success of this film

Naru:***
I’m working on some more funding  right now that’s why  it’s slow going. Everything’s been like a labor of love  out of my pocket. And Leroy put some money in as well.

I have a nonprofit, it’s called Alternative Minds Foundation and so all our stuff is going through there with this film. It’s a 501-3C so everything is a tax write off for people who want to do that.

LM:
www.alternative-minds.com

Naru:
And just later on just telling people about it when it comes out. That’s probably the best way you could help spread the word.

TR:
It sounds like these two are the right   choice for telling Joe’s story.
Leroy, through his work with Krip Hop nation, an international network of musical artists including
rappers, dj’s, producers, dancers, spoken word artists and others, all with disability; have already presented an award in recognition of Joe’s contributions. This award was presented to his family in Georgia.

Naru who had a personal relationship with Joe, while not as familiar with blindness, did gain what some may see as a simple lesson, but in fact is one that advocates have spent a life time trying to convey.

Naru:
My understanding about a person who was blind  is very limited and probably very skewed. Being around Joe was very refreshing. He was just a regular person, did regular things. Loved to joke and laugh, play tricks on you  and all of that stuff. He was just like we say, a regular Oakland Cat!
[Laughter fades out]

TR:
This is Thomas Reid,

LM:
Oh my God, this man needs to be recognized.

for Gatewave Radio.
Audio for independent living!

[Audio: Taken from Rap Battle on MTV
“There’s no charity in a rap battle!”, Sway]

TR:
The first time I thought about Hip Hop and disability was just prior to me losing my sight.  It was the fall of 2003, I believe it was MTV2 who was airing a rap battle. One of the contestants included young rapper by the name of Blind Fury.  I remember thinking his opponent was corny. He got stuck on the blind and disregarded the fury.

Blind Fury by my account was indeed better and should have won that battle.  He was more lyrical,
had a method for finding out visual details about his opponents and  he had multiple flows.  I realized the perception of Blind Fury’s talent was based on his disability.

Why would blindness limit the ability to rap? It’s vocal, what’s the big deal.
Yes, battle rap might require the ability to quickly gain information about your opponent, but Blind Fury was making that happen too.

Eventually Blind Fury took his place in history with his success on  BET’s 106 and Park’s Friday Freestyle.

[Audio: From Wild Style… “South Bronx Subway Rap”, Grandmaster Caz ]

The truth is people with disabilities have been involved with hip hop since its origins.

Leroy prior to his interest in rap was into rock and heavy metal.

LM:
Ozzie Osbourne, Metallica, ZZ Top…
***

TR:
He was then introduced to Rapper’s Delight, from the Sugar hill Gang.

[Audio: rapper’s Delight, Sugar Hill Gang]

LM:
Back then you bought the record and tried to learn all the lyrics.

This is gonna be cool!

At that time I had a walker . So picture me  with my walker going to the subway to the Bronx. Here I am this skinny guy with a walker and everybody around me has muscles,  break dancing and all that stuff.
I was just a writer back then . I dabbled in poetry.  I always told myself that I want to get in the cypher
TR:
If you’re not familiar  with the ciphers,  rappers would get together to rhyme  with one another. A time to test your newly written verse or maybe freestyle. Picture a circle of rappers passing the imaginary microphone to one another. It’s a meticulous process. You wait your turn. And you better be ready because you are going to get instant feedback on your 16 bars, or your verse. This is the place where you truly hone your skills.
While the ciphers were often about seeing who had the better skills, these
groups of mainly African American and Latino young men attracted the attention of the police.
Becoming more familiar with Leroy’s presence, he was soon declared “The  Watch Man”.

LM:
Because you’re disabled  you can watch out for the cops. The cops won’t do nothing to you . When the cops came  I used to yell you know, “po po”  and they used to scatter.  They’d just leave me there with my walker  and the cops used to get so pissed off.

TR:
Leroy played his position . He listened to more and more music.

LM:
When Run-DMC came out and did “Walk this Way”  and mixed rock with rap I was like alright this is it!

TR:
[Audio: It’s Like That, Run-DMC]

Right before I was scheduled to speak with Leroy, I read an interview he did with Daryl McDaniel’s better known as DMC of Run-DMC fame.

Now, when I heard [It’s Like That] as a young teenager, I lost my  [Censored Beep] mind!

TR in conversation with Leroy:
What was that like meeting DMC?

LM:
Oh my God, you know, I told him I grew up with you… he’s like no no we grew  up together!
For me it’s one of the highlights of my journalism career.

I saw that DMC had a book out about his depression. I also knew that back in I think the late 80’s he had a voice disability. I was like ok, DMC needs to know about Krip-Hop.

TR:
And more people need to know about Krip Hop.

In general, people are uncomfortable with disability. They don’t understand what to say to a person, how to act, maybe there’s some fear of even thinking about disability…
You know what I’m talking about because chances are you experienced it from at least one side or both.

Leroy never did participate in any of those early Bronx ciphers, but Hip Hop did get into him.

One important aspect of art and culture, is seeing yourself represented on the screen, on the canvas or stage and in the music.

As a black disabled man, that doesn’t happen that often.

LM:
My father had a huge Blues record collection and of course as we know Blues artists were blind… like Blind Willie Johnson.
[Audio: “It’s Nobody’s Fault but Mine”, Blind Willie Johnson]

My father liked Robert Winters. Robert Winters had Polio  and walked with crutches…
[Audio: “Magic Man”, Robert Winters]

Wow,  there’s disabled Black  men that do music!

I think it played a really big part of where I am today with Krip-Hop.

This year is our 10th Anniversary and we have loose chapters…

TR:
These include countries within Africa, the UK, Germany and Spain.

[Audio: “Tales of the Krip-Hop”, Rob da Noize Temple]

With the network formed by Leroy and co-founder Keith Jones, the two being disabled activists, the focus continues to be on education and advocacy.

LM:
So we saw Krip-Hop as a way to bring awareness around the history of disabled musicians from the Blues to Hip-Hop and really educate and to push the Hip-Hop arena  around Ableism thinking around disability and to really say that disabled musicians have been here since the Blues.

TR:
Krip Hop Nation produces live events featuring all sorts of artists with disabilities including; dj’s, emcee’s, spoken word artist, dancers and more.
They have put out 4 CD’s including their latest.

LM:
Our 10th Anniversary CD just came out on CDBaby.com. It has Wonder Mike  from the Sugar Hill Gang, DMC from Run-DMC.

TR:
Two names you are probably familiar with, but some might be new…like;

George Tragic
[Audio: “Industry Epidemic”, George Tragic]

Wheelchair Sports Camp

[Audio: “Hard out Here for a Gimp”, Wheelchair Sports Camp]

Toni Hickman
[Audio: “Cripple Pretty”, Toni Hickman]

Rap music and hip hop culture ironically was birthed to some degree from
exclusion and isolation.
Young kids from the South Bronx who  didn’t have access to much
including instruments so turn tables and beat boxing became its  replacements.
Barred from the downtown discos and night clubs; the community centers and parks became their place to party.

[Audio: “This Can’t Be Life”, Prinz D]

Hip Hop is a culture that created an outlet for expression.
It’s common themes consist of stories about overcoming adversity,
rebelling against  oppression, yet the disability experience goes mainly unheard.

Obviously this isn’t exclusive to rap ,
but this music with its infectious beats and rhymes is perfectly suited for Communicating all types of information with
the intention of educating.
Whether changing commonly held beliefs or getting young students to recall all types of information.

[Audio: “Hip Science”, Naru Kwina]

That’s where Naru saw a way to use his love for hip hop and combine it with his love of teaching.

While working as an assistant teacher he had the challenge of trying to teach science to kindergartners.

Naru:
The kids were like “uh!”

At recess I heard them all outside, they were singing this song off the radio; the lyrics were horrible. [Laughs…]
But, man, they knew the whole song….
And a lightbulb went off like huh!…
If I could turn these lessons into music like that and get these kids excited I wonder if they would learn these lessons like they learned that song?

So I did a series of songs  about the body and gave them to my students, the CD’s to the parents  to take home and listen to and then we did some in class. I mean they caught it so fast, it was amazing.

And so I was just using it in class and people kept telling me you need to market  this… you need to do this you need to do  that…
I ended up applying for my first grant. It’s a grant called  the Creative Work Fund. It was a partnership with this organization called the African Scientific  Institute out here in Oakland. We got the grant. $35,000 grant. I was able to produce a play, the CD and pay a lot of people in my community as well to perform  and got other artist involved to  record with me. That’s about 10 years ago. I’m still doing it to this day. Outperforming , online sales. It became half of my career. I’m still an after school teacher but I do a lot of Hip Science. I enjoy it!

TR in conversation with Naru:
What was that reaction like from the other teachers? Were they cool with this or did you get any negative feedback from them?

Naru:
They were amazed. First of all I don’t think any of them knew I rapped. I don’t know why but I kind of kept that part of my life separate  from working with the children and never realized that was one of my strengths.
I should have been using it all along.
I never even thought it would be anything like that. I just wanted my kids to learn.

TR:
And it wasn’t just his kids that were learning.
Shortly after releasing the CD series he received a call from a company interested in the product.
Naru:
This company, it’s called Overbrook Entertainment and they wanted to buy [laughter] my whole business. I’m like what? I’m not selling my business. And it turns out that was Will Smith’s company. He was in town  in San Francisco  shooting the Pursuit of Happiness  and I don’t know how  he got my CD’s  but his kids were listening  to it. I never finished the negotiations because  they were talking about they wanted to have all the marketing … I wasn’t looking to sell. It was like  this  is my baby right here!

I was like wow, I know I’m doing something now if their trying to buy  my company man! [Laughs fade away…]

***

TR:
Doing something now, well that sounds like Naru’s default mode…
He creates music with his daughter who herself is a singer and rapper at the Oakland School for the Arts.

Naru:
Matter of fact, the first song she ever wrote with me  she was 3. It was called love is the thing It’s featured on Rosie O’Donnell Family is a Family documentary. We did a video for it and everything. It was real cool!

TR:
Over several summers, the two have written a book that’s now complete and he and his daughter are creating an accompanying soundtrack.

Naru:
It’s called Panela’s Journey. It’s a very fanciful tale of a young girl who’s struggling with her identity  in the world and  her place in the world and wondering why the world is the way it is. She seeks refuge in a fanciful place.
That  one should be coming out soon as well. We’re gonna have some augmented reality, apps that go along  with the book.

TR:
Continuing to put out his own music, his latest project should be out soon.

Naru:
Naru and Strong Soul and we are The Living Room Legends!

TR:
I have some links on the blog… Reid my mind .com if you want to check out more on both Leroy and Naru.

Salute to both of these brothers for the good work their doing, truly expanding the culture.

I don’t know about you but I feel like I have to start producing some    more content!

n that note, make sure you subscribe to this podcast.
Go to your podcast app of choice and search for Reid My Mind Radio… that’s R E I D.
You can also follow me on Sound Cloud soundcloud.com/t-Reid.

[Audio: RMMRadio Theme]
Thanks for listening.

Peace!

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Reid My Mind Radio: Meet Young Ant – First Female Rapper… who’s Blind

Wednesday, February 1st, 2017

Now way back in the days when hip-hop began
With Coke LaRock,Kool Herc, and then Bam
B-boys ran to the latest jam…
– “South Bronx”, KRS One, Boogie Down Productions

I’m Old enough to remember when people not of my generation thought rap music was a fad. They never thought it would become what it is today… a worldwide billion dollar, trend setting industry. I’m sure they never thought how this art form could end up being a bridge for a 19 year old young lady adjusting to her vision loss.

Picture of Antynette, "Young Ant" in graduation cap &gown! Split image with left side featuring Young Ant sporting a t-shirt reading "No Sight" followed by a image of an Eye with a slash running through it and beneath "No Fear". The right side image is of Young Ant with the reverse side of t-shirt reading "#Team Ant".

Young Ant, is spittin’ lyrics about her own experience adjusting to blindness. And I have a feeling that’s just the beginning… Come meet the young lady and rapper! Team Ant!!!

Hit Play below and act like you know!

 

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TReid:
What’s good everybody, back this week with another episode of Reid My Mind Radio and I’m very excited to bring you this latest piece produced for Gatewave .

You may think the title says it all, but there’s more…

Take a listen and I’ll be back with some thoughts.
[“Ladies First”, Queen Latifah]
[Reid My Mind Radio Musical Intro]

TReid:
Young Ant in the building!

YA:
Young Ant in the building!

Treid:
Uh Oh!

So the way I look at this; Antynette is the person, Young Ant is the rapper!

YA:
[Laugh!] Yeah, that’s right!

TReid:
Alright, so first who is Antynette?

YA:
Antynette is a young lady who has been through a lot in a little bit over a year and half and is trying to find her through it with adjusting and coping and in different techniques that I’m learning and trying to find different avenues of expressing how I’m feeling.

[Intro to “Count your Blessings” by Young Ant]

TReid:
Beautiful!
I lost my sight about 13 years ago. And so…

YA:
Really!

TReid:
Yeh so one of the things that I like to hear from people adjusting to blindness is that they don’t first start with who they are with the fact that they are blind. You said you are a young lady!
Now, tell me who’s Young Ant?

YA:
Well Young Ant is a motivational rapper!

TReid:

Maybe that’s not what you expected to hear from an upcoming rapper.

Or perhaps your image of what it means to be blind
makes it difficult to understand how this young lady
who lost her sight only a little over a year ago can talk about counting her blessings.

Well, we’re about to challenge your perception today of both
what it means to be blind and what it means to be a rap artist.

Antynette Walker, 19 years old, lost her sight in the middle of her senior year in high school.

Marsell:
Antynette was born prematurely and she had eye surgery done on her eyes at the age of 1 to correct her vision. They told me that her eyes will be just perfectly fine; in which they was over the years.

TReid:
This is Marsell Walker, Antoinette’s mother.

At 11 years old Antynette began losing her vision.
Living in Atlanta at the time Marsell began searching for a reason for her daughter’s vision loss.

Marsell:
We started taking her to different doctors, getting different tests run and no one could tell us a reason why this was happening to her eye. They just kept prescribing different glasses for her eyes and after the years went on we just started coping with her losing vision in her left eye at the age of 11.

TReid:
In 2015 Antoinette began experiencing complications in her right eye.
Still seeking that diagnosis, the family moved to Minneapolis where she was first being treated at the University of Minnesota.

marsell:

He really didn’t see any dramatic changes within her vision from when she started seeing him. And she was going in complaining about the blurriness and spottiness and these were the same symptoms and things that she was going through at the age of 11 when she lost her vision in her left eye.

He somewhat tried to make it feel like she was hallucinating and it was all in her head and she knew off hand that it wasn’t so she asked me to get a referral to a newer doctor which is at the Mayo Clinic in Rochester.

TReid:
Seen by Ophthalmologist’s, Neurologist and other specialists at the Mayo Clinic, doctors had a very different opinion from the original doctor at the University of Minnesota.

Marsell:
That’s when they did notice her vision was changing dramatically. And he couldn’t even figure out why that previous doctor would tell us he seen no changes.

TReid:
Despite all of the tests that came back negative and the eventual diagnosis of Optic Neuropathy

Marsell:
She woke up not being able to see anything and that point he asked for us to do Steroids with Antynette for about a week… it didn’t work!

TReid:
That day she woke up blind, was Christmas 2015!

TReid in conversation with Marsell:
I mean, you’re her mom, and you’re watching your daughter lose her sight.

Marsell:
Yeh!

TReid:
What was that like for you?

Marsell:
It was really, really stressful. I have always been that parent who where if something is wrong with your kids you find a way of fixing it.
Your kids feed off of your energy, so I had to keep being positive. I’ll go in my room I’ll cry, I won’t let her know I was crying. I’ll come back out and as if nothing happened, but you know I didn’t know what to do. I was just numb!

TReid:
This was her senior year in high school.
Antoinette should have been thinking about the prom, her future.
Now she had to return to school after Christmas break, to a whole new way of life.

TReid in conversation with Young Ant:
What was that first day of school like for you?

YA:
Well, it was hard. Everything was much louder, it was just harder to navigate through crowds and different hallways. It was so much anxiety the first day going back because it was just new way of life, new environment, everything was just all brand new.

TReid in conversation with Young Ant:
What was the reaction of your classmates?

YA:
Everyone was shocked. Everyone was surprised . People more so didn’t believe it because they were just like last time I saw you you were able to see now you’re blind. More people were stand offish kind of and some people were supportive because some people knew what I was going through and knew that it was gonna happen and because we were that close and we talked about it frequently. But some were rude. I think that was mainly because they didn’t know how to take it and they didn’t know what was a proper reaction.

TReid in conversation with Young Ant:
That’s a mature response from you in terms of how you responded to those people who were being , you know, negative.

YA:
There’s going to be some people that you know, they don’t know any better or their parents didn’t teach them any better so there gonna you know make fun or say things that are inappropriate, but you gotta just learn to ignore it. Some people are for you, some people are against you. Not everyone is gonna be on your side.

[Song: “Team Ant”, by Young Ant]

TReid:
On the same side; like on a team!

Team Ant! That’s the official name of Young Ant’s crew, her support system her family.
working with her throughout this new journey.

Team Ant consist of her Dad,Aldo…

Marsell
He’s focusing on making her greater. He’s there hands on. It’s her message, but he knows a lot about rap so he has a big input on her delivery.

TReid in conversation with Marsell:
And are you playing the role of manager/marketer? What’s your role?

Marsell:
I am “Momager”

TReid in conversation with Marsell:
Momager
, ok! {Laughs}

Marsell:
[Laughs] It’s a new word for me

TReid in conversation with Marsell
I like it!

Marsell:
Hooking up photo shoots and videos hooking up studio time and reaching out to different people to try and get her story out there. And her father is the one that comes and oversee everything and makes sure it sounds right.

TReid::
The oldest of 4 siblings, setting an example for them is really important to Antynette.
She’s working hard at improving all of her skills. That’s Braille, navigating with her white cane, independent living skills and learning to use a screen reader and computer.

Traditionally, One of the most important aspects of being a rapper is writing your own rhymes.
At least, if you want any true rap Aficionado to take you seriously.

I had to ask…

TReid in conversation with Young Ant:
Are you writing your own rhymes right now?

YA:
Yeh!

TReid in conversation with Young Ant:
You’re like yehhhh!

YA:
[Laughs]

TReid in conversation with Young Ant:
How do you feel about the writing? Does that mean something to you as opposed to having others write your rhymes?

YA:
Yeh, Because before I went blind I was a big writer. I wanted to be a novelist. I used to write short stories and poems and different things of that sort. So I feel like you know with me losing my sight it doesn’t mean that have to stop doing what I love doing. Now I have to be more repetitive when I’m writing the stuff so I can remember it.

TReid:
In any art form, early influences can help develop an artist’s own unique style.

YA:
My father is a rapper so I kind of grew up around music and rap music. Growing up around him, listening to him rap. Growing up in Atlanta, Georgia I just grew up listening to it. Artists like Biggie Smalls, Tupac and Run-DMC and you know Snoop Dogg

TReid in conversation with Young Ant:
Very nice!.
See, I made my kids, both of them, they had to learn some early Run-DMC… I’d make them learn the lyrics…

YA:
Laughs…

TReid in conversation with Young Ant:
For real! I ain’t joking!

YA:
Right, get to the roots!

TReid:
Based on the artists mentioned I’d say Young Ant has some knowledge of rap music’s pioneers. She likes lyricists, music with a message and showmanship.

YA:
I like to call myself a motivational rapper. I’m mainly aiming to inspire, to motivate, to let everyone know that no matter what you’re going through and no matter what happens that doesn’t mean that your life stops just because you’re diagnosed with a certain thing or something traumatic happens in your life. People in society tell you that you can no longer go on. You can be whatever you want to be and you can do whatever you want to do if you set your mind to it. All my music is positive and clean. You know fun, uplifting and motivational.

TReid:
She’s gearing up for some live performances later this year. Like the South by Southwest festival in Austin Texas and Coast to Coast in Atlanta.

TReid in conversation with Young Ant:
How do you navigate the stage?

YA:
Usually, I go on before to get a feel for the stage you know to see how big it is to see what I’m working with. And then you know once I get a feel for how big or small it is , I kind of just you know [exhale!] let loose!

TReid:
Young Ant is just getting started and open to collaborating with other artists.

YA:
I would love to do a song with Stevie Wonder. That’s like the top of my list.

TReid in conversation with Young Ant:
Hold on, you’re a Stevie fan too!

YA:
Whatttttt?

TReid in conversation with Young Ant:
You’ve always been a Stevie fan?
I love Stevie… yeh! Even before…

TReid in conversation with Young Ant:
Now I’m gonna test you. You’re talking to a real Stevie head right now. Tell me what you like. Give me a song.

YA:
[Sings Isn’t she lovely, isn’t she wonderful]

TReid in conversation with Young Ant:
Ok!

YA:
I like Superstitious! That’s that’s my jam!

TReid:
There’s definitely something wonderful about this young lady.
Maybe it’s the inner strength that shines through her words and personality.
The determination that’s helping her adjust to blindness and pursue her goals.
She has the courage to make her way in quite honestly what’s a male and able bodied dominated genre
in the entertainment industry
which by the way, has never been that open to disability.

Young Ant though has a team.

[Song: “Team Ant”, by Young Ant]

A support system that’s lead by the two people who love her most, mom and dad.

[Song: “Count your Blessing” by Young Ant]

That’s an asset whether adjusting to blindness or starting a music career.

To listen to this track called Count your Blessings go to Sound Cloud and follow her on social media.

Let them know Momager!

Marsell:
Young Ant, first blind female rapper. You can find her on YouTube as Young ANT. On Twitter , Sound Cloud, Instagram as YoungAnt1121. Her Facebook page is Team Ant.

I’m Thomas Reid…

[Audio YA: I kind of just you know, let loose!]

TReid:
For Gatewave Radio, Audio for Independent Living!

[Sound of Record rewind]
This is why I like producing this podcast.

As a father of two incredibly gifted, intelligent and beautiful young ladies I was drawn to this story.

I understand the value of speaking with someone who has walked in your shoes.

Graduating high school is the time when you look to a future hopefully full of opportunity
. For Young Ant and anyone faced with the loss of their sight or any disability for that matter,
it’s natural to think that the opportunity has faded away.

All it takes though, is a glimpse of chance or hope to peek through.

That could be a small success.

Young Ant is only one year into her adjustment process.
Honestly, to some extent I think that process is lifelong. Not like a life sentence, but rather like a commitment.
A commitment to living the best life possible;
seeing happiness not as a destination but a daily process.

Now, you know what’s not a daily process?
subscribing to this podcast, Reid My Mind Radio…
For real though! All it takes is a couple of steps;
go to your podcast app, search for Reid My Mind Radio… that’s R E I D
and then hit subscribe.

Then become a fan!
I ‘m talking about young ant, but feel free to become a fan of the podcast too!

Seriously, I hope you all heard the character, strength and maturity like I did and become a fan of both the young lady, Antynette and of course, the rapper Young Ant!

[Song Roxanne Shante: “Got the party people screaming… “Go on Girl.!”… from “Have a Nice Day”}
Reid My Mind Outro Music

TReid:
Peace!

Peace!

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